Ireland
--:--IST
Starting soon Not applicable

Peripheral Venous Catheter Infiltration and Extravasation

NCT07545031 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-04-27
Last updated
2026-04-22

Condition(s) studied

Infiltration of Peripheral IV TherapyExtravasation

Investigational drug(s) / intervention(s)

video-assisted peripheral venous catheter infiltration and extravasation training

video-assisted peripheral venous catheter infiltration and extravasation training: Educational videos on infiltration and extravasation will be prepared by the researcher based on a comprehensive literature review. First, an in-depth review will be conducted; then, a written script will be developed. The video will include eight sections: definition, epidemiology, risk factors, signs and symptoms, diagnosis, prevention, treatment, and the nurse's role. It will be narrated by the researcher and include slides, simulated demonstrations in a skills laboratory, and animations created with support from a graphic design specialist. The final video will be developed under expert consultation, submitted for review, and shared via a QR code in the thesis.,

Study summary

This study aims to evaluate the effect of video-supported education, prepared for pediatric nurses, on their knowledge, attitudes, and perceived professional competence regarding peripheral venous catheter (PVC) infiltration and extravasation. The research will be conducted as a parallel-group, randomized controlled experimental design, involving pre-test and post-test measurements. The study will be carried out with nurses working in the pediatric clinics of Konya Dr. Ali Kemal Belviranlı Women's Health and Pediatric Hospital.

During the data collection process, a Descriptive Information Form, an Infiltration and Extravasation Knowledge Questionnaire, an Attitude Scale Towards Preventing Infiltration and Extravasation, and a Competency Scale for Clinical Nurses will be utilized. Nurses in the intervention group will receive video-supported education on peripheral venous catheter infiltration and extravasation, which will be prepared by the researchers with expert consultation. No intervention will be applied to nurses in the control group. Pre-test data will be collected face-to-face from both the intervention and control groups within one week prior to the intervention, and post-test data will be collected one month after the intervention.

The findings are expected to improve nurses' knowledge and attitudes towards complications they may encounter in PVC applications, enhance patient safety in clinical practice, and provide evidence-based contributions to nursing education. In these respects, the study aims to make a significant contribution to the literature and pediatric nursing practice.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Having worked as a pediatric nurse for at least 6 months. Exclusion Criteria: * Being on long-term leave (maternity leave, unpaid leave, sick leave, etc.), * Refusal to participate in work.

Primary outcome measure(s)

  • Descriptive Information Form — Pre-test (before the video-assisted peripheral venous catheter infiltration and extravasation training), post-test (1 month after the video-assisted peripheral venous catheter infiltration and extravasation training).
    The Descriptive Information Form was developed by the researchers based on similar studies in the literature (Orman et al., 2022; Tok Yıldız \& Avcı, 2019). It consists of 11 questions aimed at identifying nurses' personal and professional characteristics, including age, gender, education level, average number of patients cared for, having children, monthly working pattern, and experience with infiltration and extravasation cases.

Trial sites (1)

FacilityCityRegionStatus
Selcuk University Faculty of Nursing Konya Konya
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07545031 on ClinicalTrials.gov ↗ ← All trials in Turkey